Answer Posted / sameer jagtap
its standard format of SOP for the preparation of new SOP
| Is This Answer Correct ? | 0 Yes | 0 No |
Post New Answer View All Answers
Did anybody have method for acetyl cysteine effervescnce tablet
Is it nessesary all multimedia dissolution require descriminatory?
what is the acceptance criteria for enteric coated tablets in 0.1n hcl validation in each parameter?
If we do accuracy at same concentration at which linearity planned,what is the need to do linearity separately?
In BP2013, Loperamid HCl monograph. Assay by titration with 0.1N sodium hydroxide using hydrocloric acid 0.01N and reading the volume added between the 2 points of inflexion. I have a question that if the diluent solvent is ethanol is certainly consumed a amount of volume of titrant, so this volume must be eliminated on the result calculation or not apart from first point which is subtracted above.
In which situation we require to prepare the standard solution from sample in Related substance method?
what is mean by covalidation
pharma industries oriented
what parameters we will consider while developing a HPLC method and how we confirm our HPLC method is valid?
give clarity of linearity and range in method validation
why holium oxide prepared in 10% HCLO4 SOLUTION
in which situation ion pair agent require to use?
what are the guidelines for analytical method validations?
if you get peak in blank then what require to do?
Ratio of Water and Acetonitrile(diluent) is not recommended to use in cleaning method validation,why?